FDA 510(k) Application Details - K170961

Device Classification Name	More FDA Info for this Device
510(K) Number	K170961
Device Name	NuVasive CoRoent Small Interlock II System
Applicant	NuVasive, Incorporated 7475 Lusk Blvd. San Diego, CA 92121 US Other 510(k) Applications for this Company
Contact	Cynthia Adams Other 510(k) Applications for this Contact
Regulation Number	More FDA Info for this Regulation Number
Classification Product Code	OVE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/31/2017
Decision Date	06/08/2017
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OR - Orthopedic
Review Advisory Committee	OR - Orthopedic
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review